Category Archives: Food & Drug Recalls

FDA approves first drug for reducing the risk of sexually acquired HIV infection

Today, the U.S. Food and Drug Administration approved Truvada (emtricitabine/tenofovir disoproxil fumarate), the first drug approved to reduce the risk of HIV infection in uninfected individuals who are at high risk of HIV infection and who may engage in sexual activity with HIV-infected partners.

SUPPLIER RECALLS MEATBALL ITEMS SOLD THROUGH DELI

SCARBOROUGH, Maine – Hannaford Supermarkets today alerted customers to a recall issued by New Jersey-based Buona Vita Inc. of three meatball products, due to possible contamination with Listeria monocytogenes.The three products are all sold through the deli department: Homestyle Meatballs with Sauce, sold by the pound; Meatball Panini – cold, UPC # 941260723096; and Meatball Panini – hot, UPC # 94126072102.

PMI Nutrition International Initiates Voluntary Recall of AquaMax Products; Expands Voluntary Recall of Mazuri and LabDiet Feed Products Due to Potential Elevated Vitamin D Level

PMI Nutrition International is initiating a voluntary recall of certain varieties of the AquaMax™ feed products with specific lot codes listed below, due to the potential for elevated vitamin D levels. Although no customer complaints have been received to date, the products are being recalled due to analytical test results that indicate a potential for elevated levels of vitamin D.

Hospira Announces A Nationwide Recall of Certain Lots of Injectable Carboplatin, Cytarabine, Paclitaxel and Methotrexate Due to Glass Vial Defect

Hospira, Inc. (NYSE: HSP), the world’s leading provider of injectable drugs and infusion technologies, issued this press release today to further inform the general public about a previously communicated user level recall of a total of 19 lots of carboplatin, cytarabine, paclitaxel, and methotrexate (see table below) in the United States due to visible particles embedded in the glass located at the neck of the vial. There may be potential for product to come into contact with the embedded particles and the particles may become dislodged into the solution.

Voluntary Recall of Feed Solutions Feed Products Due to Potential Elevated Vitamin D Level

Feed Solutions has initiated a voluntary recall of certain varieties of the feed products with specific lot codes listed below, due to the potential for elevated vitamin D levels. Elevated vitamin D levels may cause death or otherwise be harmful to animals and fish if fed for extended periods, potentially resulting in lack of interest in eating, weight loss and possible joint stiffness.

FDA seeks to halt production, distribution of dietary supplements at NY company

The U.S. Food and Drug Administration is seeking an injunction requiring Kabco Pharmaceuticals Inc., and owner Abu Kabir, of Amityville, N.Y., to stop producing and distributing dietary supplements until they comply with the Federal Food, Drug and Cosmetic Act and current good manufacturing practice (cGMP) requirements for dietary supplements.